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Genetic Diversity Among SARS-CoV2 Strains in South America may Impact Performance of Molecular Detection

机译:南美洲的SARS-COV2菌株中的遗传多样性可能会影响分子检测的性能

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摘要

Since its emergence in Wuhan (China) on December 2019, the Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) has rapidly spread worldwide. After its arrival in South America in February 2020, the virus has expanded throughout the region, infecting over 900,000 individuals with approximately 41,000 reported deaths to date. In response to the rapidly growing number of cases, a number of different primer-probe sets have been developed. However, despite being highly specific, most of these primer-probe sets are known to exhibit variable sensitivity. Currently, there are more than 300 SARS-CoV2 whole genome sequences deposited in databases from Brazil, Chile, Ecuador, Colombia, Uruguay, Peru, and Argentina. To test how regional viral diversity may impact oligo binding sites and affect test performance, we reviewed all available primer-probe sets targeting the E, N, and RdRp genes against available South American SARS-CoV-2 genomes checking for nucleotide variations in annealing sites. Results from this in silico analysis showed no nucleotide variations on the E-gene target region, in contrast to the N and RdRp genes which showed massive nucleotide variations within oligo binding sites. In lines with previous data, our results suggest that the E-gene stands as the most conserved and reliable target when considering single-gene target testing for molecular diagnosis of SARS-CoV-2 in South America.
机译:自2019年12月在武汉(中国)出现以来,严重急性呼吸综合征冠状病毒2(SARS-COV-2)迅速传播全球。在2020年2月抵达南美洲后,病毒在整个地区扩大,感染了超过900,000人,约有41,000人报告的死亡日期。响应于越来越快地的情况,已经开发了许多不同的引物探针组。然而,尽管是高度特异性的,但是已知大多数这些引物探针组表现出可变灵敏度。目前,存在超过300多个SARS-COV2全基因组序列,沉入巴西,智利,厄瓜多尔,哥伦比亚,乌拉圭,秘鲁和阿根廷。为了测试区域病毒多样性如何影响寡核苷酸结合位点并影响测试性能,我们审查了针对可用南美SAR-COV-2基因组的所有可用的底漆探针组针对E,N和RDRP基因进行检查检查退火部位的核苷酸变化。由其在硅分析中的结果显示,与在寡核苷酸结合位点内显示出大量核苷酸变化的N和RDRP基因,没有对E-Gene靶区域的核苷酸变化没有核苷酸变化。我们的结果表明,当考虑南美洲SARS-COV-2的单一基因靶标测试时,E-基因的目标是最保守和可靠的目标。

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